HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161975Generated: October 29, 2026
Ammonia → 11beta-Methyl 17beta-hydroxyestr-5(10)-en-3-one
https://huagongshe.com/reaction/1161975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Lithium ammonia | HCID 57431548 | — |
| Reactant | 11beta-Methyl-17beta-hydroxyestra-4,9-diene | HCID 68648355 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 11beta-Methyl 17beta-hydroxyestr-5(10)-en-3-one | HCID 86621277 | 100% |
Reaction Steps
Under an argon atmosphere, lithium wire (270 mg, 38.9 mmol), cut into small pieces, was added to anhydrous ammonia (200 mL) and stirred at reflux for 2 hr. The lithium/ammonia mixture was chilled to −78° C. and a THF solution of the dienone (5a, 4.03 g, 14.07 mmol) containing t-butanol (1.24 mL), was added over 15 min. The mixture was stirred at −78° C. for 15 min before excess of lithium was destroyed with isoprene (1.5 mL). The reaction was quenched by means of the addition of solid ammonium chloride (16 g, 296.3 mmol). Ammonia was allowed to evaporate under a constant stream of nitrogen. The THF layer was washed with H2O and brine. The aqueous washes were extracted with ether (2×200 mL). the combined organic extracts were dried over Na2SO4 and evaporation of the solvent gave 4.25 g of 6a as a white solid in 100% yield. NMR (300 MHz, CDCl3): δ 0.889 (s, 3H, C18-7CH3), 0.916 (d, 3H, C11β-CH3), and 3.655 (t, 1H, C17β-H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820642B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-a8f3622d17454de88e89e3f6d72195e8 |
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| Source note | uspto-grants-2010_10 |
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